Adatare Denis Nyabire, Kraemer Florian, Agyeman Mary Ann, Agbemavi-Kudiafia Lois Afia, Tenkorang Pearl Ohenewaa, Patel Krishi, Adjei Osei Emmanuel Kwadwo, Awindaogo Joseph Kebo, Darko Kwadwo, Ametefe Mawuli
Neurosurgery Department, Korle Bu Teaching Hospital, Accra, Ghana.
Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.
Ann Med Surg (Lond). 2025 May 30;87(7):4597-4601. doi: 10.1097/MS9.0000000000003374. eCollection 2025 Jul.
Complex cranial anatomy can lead to unique and severe complications, such as the uncommon simultaneous presentation of an epidural abscess (EDA), cranial osteomyelitis, and spontaneous epidural hematoma (SEDH), posing potential diagnostic and management challenges.
We present the case of a 15-year-old boy who presented with a 2-week history of headaches and painless swelling of the right eye accompanied by fever, poor appetite, and intermittent nasal discharge over 2 months. A computed tomography scan revealed a hypodense and hyperdense biconvex frontal region collection with an associated subgaleal collection thought to be an abscess. Emergency craniectomy, abscess drainage, and osteomyelitic bone removal were also performed. Intraoperatively, the hematoma and EDA were evacuated. Postoperatively, the patient showed rapid clinical improvement by day 1 and completed a 3-week course of intravenous antibiotics. The patient was subsequently discharged with no neurological deficits, a well-healed surgical site, and plans for follow-up and skull defect repair.
The rarity of this condition accounts for the lack of established prevalence data. It may contribute to uncertainty in management; however, a standard approach incorporating thorough clinical assessment, imaging, and surgical intervention can lead to favorable clinical outcomes for patients.
The rare occurrence of SEDH in association with EDA and cranial osteomyelitis poses significant challenges for clinicians in achieving early diagnosis. This delay can have serious implications for the patients. Therefore, it is crucial for clinicians to be aware of these peculiarities.
复杂的颅骨解剖结构可导致独特且严重的并发症,例如硬膜外脓肿(EDA)、颅骨骨髓炎和自发性硬膜外血肿(SEDH)罕见地同时出现,给诊断和治疗带来潜在挑战。
我们报告一例15岁男孩的病例,他有2周头痛病史,右眼无痛性肿胀,并伴有发热、食欲减退以及2个月来的间歇性流涕。计算机断层扫描显示额部区域有一个低密度和高密度的双凸形病灶,伴有一个被认为是脓肿的帽状腱膜下病灶。还进行了急诊颅骨切除术、脓肿引流和骨髓炎骨质清除术。术中,清除了血肿和硬膜外脓肿。术后,患者在第1天临床症状迅速改善,并完成了为期3周的静脉抗生素治疗疗程。患者随后出院,无神经功能缺损,手术部位愈合良好,并制定了随访和颅骨缺损修复计划。
这种情况的罕见性导致缺乏确切的患病率数据。这可能导致治疗的不确定性;然而,采用全面临床评估、影像学检查和手术干预的标准方法可为患者带来良好的临床结局。
自发性硬膜外血肿与硬膜外脓肿和颅骨骨髓炎同时出现的罕见情况给临床医生实现早期诊断带来了重大挑战。这种延误可能对患者产生严重影响。因此,临床医生了解这些特殊情况至关重要。